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X-WR-CALNAME:Bordeaux Neurocampus
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X-WR-CALDESC:Évènements pour Bordeaux Neurocampus
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DTSTART:20191027T010000
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DTSTART;TZID=Europe/Paris:20190503T100000
DTEND;TZID=Europe/Paris:20190503T113000
DTSTAMP:20260315T054749
CREATED:20190305T114303Z
LAST-MODIFIED:20200316T134726Z
UID:103907-1556877600-1556883000@www.bordeaux-neurocampus.fr
SUMMARY:Séminaire impromptu - Maxime Assous
DESCRIPTION:\n	\n		\n			Lieu : CGFB \n\nMaxime Assous\nMaxime ASSOUS\nCenter For Molecular and Behavioral Neurosciences\nRutgers University\nNewark\, New Jersey\, USA \nInvitants : Jérôme Baufreton / Nicolas Mallet\nIMN \n\n		\n	\n\n	\n		\n			Abstract\nThe classical view on striatal GABAergic interneuron function has been that they operate as independent\, parallel\, feed-forward inhibitory elements providing inhibitory inputs to SPNs. Much recent evidence has shown that the extrinsic innervation of striatal interneurons is not indiscriminate but rather very specific\, and that striatal interneurons are themselves interconnected in a cell-type-specific manner. This suggests that the impact of extrinsic inputs on striatal neuronal activity critically depends on synaptic interactions within interneuronal circuitry. For instance\, we recently described the existence of a striatal GABAergic interneuron population (Spontaneously Active Bursty Interneuron; SABIs)\, receiving cortical and thalamic innervation\, which does not seem to innervate the projection neurons\, indicating that it may represent the first interneuron-selective interneuron in striatum. Furthermore\, we recently showed that the most common response of low threshold spiking interneurons (LTSI) to thalamic stimulation is a disynaptic inhibition through thalamic activation of tyrosine hydroxylase-expressing interneurons (THINs). Further investigation of the excitatory innervation of striatal interneurons show cell-type specific disynaptic inhibitory responses after engagement of the cortex or the thalamus suggesting a high specificity and selectivity in the striatal microcircuitry. In addition\, our recent data suggest the existence of a novel source of glutamatergic innervation to the striatum\, originating in the pedunculopontine nucleus which selectively targets striatal interneurons\, inhibiting the striatal output via feedforward inhibition. Understanding the local striatal connectivity is fundamental to comprehend the integration of the different extrinsic inputs to the striatum. \nSelected publications :\nAssous M\, Faust TW\, Assini R\, Shah F\, Sidibe Y\, Tepper JM. (2018) Identification and Characterization of a Novel Spontaneously Active Bursty GABAergic Interneuron in the Mouse Striatum. J Neurosci. 2018 Jun 20;38(25):5688-5699. doi: 10.1523/JNEUROSCI.3354-17.2018. Epub 2018 May 22 \nAssous M\, Tepper JM. (2018) Excitatory extrinsic afferents to striatal interneurons and interactions with striatal microcircuitry. Eur J Neurosci. 2018 Feb 26. doi: 10.1111/ejn.13881. \nAssous M\, Kaminer J\, Shah F\, Garg A\, Koós T\, Tepper JM. (2017) Differential processing of thalamic information via distinct striatal interneuron circuits.Nat Commun. 2017 Jun 12;8:15860. doi: 10.1038/ncomms15860. \n\n		\n	\n\n
URL:https://www.bordeaux-neurocampus.fr/event/seminaire-impromptu-maxime-assous/
CATEGORIES:A la une,Pour les scientifiques,Séminaire Impromptu
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